Characterization of proteomic profile of the replication complex associated with the yellow fever virus

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Authors

D. Auganova

National Center of Biotechnology, Astana, 010000, Kazakhstan

B. Ingirbay

National Center of Biotechnology, Astana, 010000, Kazakhstan

A. Shustov

National Center of Biotechnology, Astana, 010000, Kazakhstan

P. Tarlykov

National Center of Biotechnology, Astana, 010000, Kazakhstan

Abstract

Background: The yellow fever virus is an RNA virus from the Flaviviridae genus, which includes over 70 pathogenic species. This research aims to describe how to characterize the proteomic composition of the yellow fever virus replication system. The YFV genome encodes a polyprotein made of structural and non-structural (NS) proteins; the latter are essential for starting the replication complex.

Materials and methods: The yellow fever virus (YFV) replication complex was modified and labeled with green fluorescence protein (GFP) to help identify proteins involved in virus replication and their compartments. Afterwards, the YFV-GFP construct was used to infect mammalian cells, which were then cultivated to collect a biomass of 0.5-1 g infected cells in total. Intercellular fractions were extracted using ultracentrifugation in a sucrose density gradient fractionation. Anti-GFP immunoaffinity chromatography was conducted using sorbents containing anti-GFP antibodies, following the proteolytic digestion and LC-MS/MS tandem mass spectrometry analysis in the Impact II (Bruker Daltonics) mass spectrometry.

Results: Protein profiles of the construction searched in the Mascot server via the NCBI database and SwissProt. Identified the proteins involved in the replication process, such as genomic polyprotein (POLG), non-structural protein 1 (NS-1), non-structural protein (NS-2), as well as GFP. Besides, host hamster proteins were extracted and identified among the YFV proteins.

Conclusion: The described approach, represented using the yellow fever virus, shows an adaptable method which can be applied to various viruses and plays a significant role in the development of effective target therapies against viruses.

Acknowledgement: This research was funded by the Science Committee of the Ministry of Science and Higher Education of the Republic of Kazakhstan (Grant No. AP23488393).

Key words: Yellow fever virus, genetic engineering, proteomics, mass-spectrometry

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